-
1
-
-
0038795172
-
Genetics of melanoma predisposition
-
Hayward NK. Genetics of melanoma predisposition. Oncogene 2003;22:3053-62
-
(2003)
Oncogene
, vol.22
, pp. 3053-3062
-
-
Hayward, N.K.1
-
2
-
-
0029664339
-
Germline mutations in the p16INK42 binding domain of CDK4 in familial melanoma
-
Zuo L, Weger J, Yang Q, Goldstein AM, Tucker MA, Walker GJ, et al. Germline mutations in the p16INK42 binding domain of CDK4 in familial melanoma. Nat Genet 1996;12:97-9
-
(1996)
Nat Genet
, vol.12
, pp. 97-99
-
-
Zuo, L.1
Weger, J.2
Yang, Q.3
Goldstein, A.M.4
Tucker, M.A.5
Walker, G.J.6
-
3
-
-
6844226190
-
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France
-
Soufir N, Avril MF, Chompret A, Demenais F, Bombled J, Spatz A, et al. Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group. Hum Mol Genet 1998;7:209-16
-
(1998)
The French Familial Melanoma Study Group. Hum Mol Genet
, vol.7
, pp. 209-216
-
-
Soufir, N.1
Avril, M.F.2
Chompret, A.3
Demenais, F.4
Bombled, J.5
Spatz, A.6
-
4
-
-
0034230515
-
New developments in melanoma genetics
-
Hayward N. New developments in melanoma genetics. Curr Oncol Rep 2000;2:300-6
-
(2000)
Curr Oncol Rep
, vol.2
, pp. 300-306
-
-
Hayward, N.1
-
5
-
-
68149179663
-
Genome-wide association study identifies three loci associated with melanoma risk
-
Bishop DT, Demenais F, Iles MM, Harland M, Taylor JC, Corda E, et al. Genome-wide association study identifies three loci associated with melanoma risk. Nat Genet 2009;41:920-8
-
(2009)
Nat Genet
, vol.41
, pp. 920-928
-
-
Bishop, D.T.1
Demenais, F.2
Iles, M.M.3
Harland, M.4
Taylor, J.C.5
Corda, E.6
-
6
-
-
11144298761
-
Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi
-
Gandini S, Sera F, Cattaruzza MS, Pasquini P, Abeni D, Boyle P, et al. Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi. Eur J Cancer 2005;41:28-44
-
(2005)
Eur J Cancer
, vol.41
, pp. 28-44
-
-
Gandini, S.1
Sera, F.2
Cattaruzza, M.S.3
Pasquini, P.4
Abeni, D.5
Boyle, P.6
-
7
-
-
0035260890
-
IL-10 promoter polymorphisms influence tumour development in cutaneous malignant melanoma
-
Howell WM, Turner SJ, Bateman AC, Theaker JM. IL-10 promoter polymorphisms influence tumour development in cutaneous malignant melanoma. Genes Immun 2001;2:25-31
-
(2001)
Genes Immun
, vol.2
, pp. 25-31
-
-
Howell, W.M.1
Turner, S.J.2
Bateman, A.C.3
Theaker, J.M.4
-
8
-
-
70349977810
-
DNA repair gene polymorphisms and risk of cutaneous melanoma: A systematic review and meta-analysis
-
Mocellin S, Verdi D, Nitti D. DNA repair gene polymorphisms and risk of cutaneous melanoma: A systematic review and meta-analysis. Carcinogenesis 2009;30:1735-43
-
(2009)
Carcinogenesis
, vol.30
, pp. 1735-1743
-
-
Mocellin, S.1
Verdi, D.2
Nitti, D.3
-
9
-
-
0029156961
-
Phenotype of glutathione S-transferase Mu (GSTM1) and susceptibility to malignant melanoma
-
Lafuente A, Molina R, Palou J, Castel T, Moral A, Trias M. Phenotype of glutathione S-transferase Mu (GSTM1) and susceptibility to malignant melanoma. Br J Cancer 1995;72:324-6
-
(1995)
Br J Cancer
, vol.72
, pp. 324-326
-
-
Lafuente, A.1
Molina, R.2
Palou, J.3
Castel, T.4
Moral, A.5
Trias, M.6
-
10
-
-
17544392528
-
Vitamin D receptor polymorphisms are associated with altered prognosis in patients with malignant melanoma
-
Hutchinson PE, Osborne JE, Lear JT, Smith AG, Bowers PW, Morris PN, et al. Vitamin D receptor polymorphisms are associated with altered prognosis in patients with malignant melanoma. Clin Cancer Res 2000;6:498-504
-
(2000)
Clin Cancer Res
, vol.6
, pp. 498-504
-
-
Hutchinson, P.E.1
Osborne, J.E.2
Lear, J.T.3
Smith, A.G.4
Bowers, P.W.5
Morris, P.N.6
-
11
-
-
69949165787
-
Distal and proximal interleukin (IL)-10 promoter polymorphisms associated with risk of cutaneous melanoma development: A case-control study
-
Schoof N, von Bonin F, König IR, Mössner R, Krüger U, Reich K, et al. Distal and proximal interleukin (IL)-10 promoter polymorphisms associated with risk of cutaneous melanoma development: A case-control study. Genes Immun 2009;10: 586-90
-
(2009)
Genes Immun
, vol.10
, pp. 586-590
-
-
Schoof, N.1
Von Bonin, F.2
König, I.R.3
Mössner, R.4
Krüger, U.5
Reich, K.6
-
12
-
-
77952389202
-
Genetics of pigmentation and melanoma predisposition
-
Pho LN, Leachman SA. Genetics of pigmentation and melanoma predisposition. G Ital Dermatol Venereol 2010;145: 37-45
-
(2010)
G Ital Dermatol Venereol
, vol.145
, pp. 37-45
-
-
Pho, L.N.1
Leachman, S.A.2
-
13
-
-
0036789853
-
Melanoma and human leukocyte antigen status: The missing link?
-
Sondak VK, Chang AE. Melanoma and human leukocyte antigen status: The missing link? Ann Surg Oncol 2002;9: 723-4
-
(2002)
Ann Surg Oncol
, vol.9
, pp. 723-724
-
-
Sondak, V.K.1
Chang, A.E.2
-
14
-
-
69449101795
-
Genome-wide associations: Studies for melanoma and nevi
-
Yeh I, Bastian BC. Genome-wide associations: Studies for melanoma and nevi. Pigment Cell Melanoma Res 2009;22: 527-8
-
(2009)
Pigment Cell Melanoma Res
, vol.22
, pp. 527-528
-
-
Yeh, I.1
Bastian, B.C.2
-
15
-
-
72449211941
-
Identification of modifier genes for cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations
-
Yang XR, Pfeiffer RM, Wheeler W, Yeager M, Chanock S, Turner MA, et al. Identification of modifier genes for cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations. Int J Cancer 2009;125: 2912-7
-
(2009)
Int J Cancer
, vol.125
, pp. 2912-2917
-
-
Yang, X.R.1
Pfeiffer, R.M.2
Wheeler, W.3
Yeager, M.4
Chanock, S.5
Turner, M.A.6
-
16
-
-
65649118981
-
Melanoma genetics: An update on risk-associated genes
-
Udayakumar D, Tsao H. Melanoma genetics: An update on risk-associated genes. Hematol Oncol Clin North Am 2009;23: 415-29
-
(2009)
Hematol Oncol Clin North Am
, vol.23
, pp. 415-429
-
-
Udayakumar, D.1
Tsao, H.2
-
19
-
-
10644297320
-
Genetics in melanoma
-
Stahl S, Bar-Meir E, Friedman E, Regev E, Orenstein A, Winkler E. Genetics in melanoma. Isr Med Assoc J 2004;6:774-7
-
(2004)
Isr Med Assoc J
, vol.6
, pp. 774-777
-
-
Stahl, S.1
Bar-Meir, E.2
Friedman, E.3
Regev, E.4
Orenstein, A.5
Winkler, E.6
-
20
-
-
0038819652
-
The INK4a/ARF locus and melanoma
-
Sharpless NE, Chin L. The INK4a/ARF locus and melanoma. Oncogene 2003;22:3092-8
-
(2003)
Oncogene
, vol.22
, pp. 3092-3098
-
-
Sharpless, N.E.1
Chin, L.2
-
21
-
-
0028100903
-
Germline p16 mutations in familial melanoma
-
Hussussian CJ, Struewing JP, Goldstein AM, Higgins PA, Ally DS, Sheahan MD, et al. Germline p16 mutations in familial melanoma. Nat Genet 1994;8:15-21
-
(1994)
Nat Genet
, vol.8
, pp. 15-21
-
-
Hussussian, C.J.1
Struewing, J.P.2
Goldstein, A.M.3
Higgins, P.A.4
Ally, D.S.5
Sheahan, M.D.6
-
22
-
-
0028085975
-
Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus
-
Kamb A, Shattuck-Eidens D, Eeles R, Liu Q, Gruis NA, Ding W, et al. Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nat Genet 1994;8:23-6
-
(1994)
Nat Genet
, vol.8
, pp. 23-26
-
-
Kamb, A.1
Shattuck-Eidens, D.2
Eeles, R.3
Liu, Q.4
Gruis, N.A.5
Ding, W.6
-
23
-
-
0029562169
-
Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds
-
Holland EA, Beaton SC, Becker TM, Grulet OM, Peters BA, Rizos H, et al. Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds. Oncogene 1995;11:2289-94
-
(1995)
Oncogene
, vol.11
, pp. 2289-2294
-
-
Holland, E.A.1
Beaton, S.C.2
Becker, T.M.3
Grulet, O.M.4
Peters, B.A.5
Rizos, H.6
-
24
-
-
0028981664
-
Germline p16INK4A mutation and protein dysfunction in a family with inherited melanoma
-
Liu L, Lassam NJ, Slingerland JM, Bailey D, Cole D, Jenkins R, et al. Germline p16INK4A mutation and protein dysfunction in a family with inherited melanoma. Oncogene 1995;11: 405-12
-
(1995)
Oncogene
, vol.11
, pp. 405-412
-
-
Liu, L.1
Lassam, N.J.2
Slingerland, J.M.3
Bailey, D.4
Cole, D.5
Jenkins, R.6
-
25
-
-
0028971713
-
Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds
-
Walker GJ, Hussussian CJ, Flores JF, Glendening JM, Haluska FG, Dracopoli NC, et al. Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds. Hum Mol Genet 1995; 4:1845-52
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1845-1852
-
-
Walker, G.J.1
Hussussian, C.J.2
Flores, J.F.3
Glendening, J.M.4
Haluska, F.G.5
Dracopoli, N.C.6
-
26
-
-
0028121279
-
A cell cycle regulator potentially involved in genesis of many tumor types
-
Kamb A, Gruis NA, Weaver-Feldhaus J, Liu Q, Harshman K, Tavtigian SV, et al. A cell cycle regulator potentially involved in genesis of many tumor types. Science 1994;264:436-40
-
(1994)
Science
, vol.264
, pp. 436-440
-
-
Kamb, A.1
Gruis, N.A.2
Weaver-Feldhaus, J.3
Liu, Q.4
Harshman, K.5
Tavtigian, S.V.6
-
27
-
-
0029102927
-
Brief Report a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene
-
Whelan AJ, Bartsch D, Goodfellow PJ. Brief Report: A familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene. N Engl J Med 1995;333:975-7
-
(1995)
N Engl J Med
, vol.333
, pp. 975-977
-
-
Whelan, A.J.1
Bartsch, D.2
Goodfellow, P.J.3
-
28
-
-
0029129816
-
Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations
-
Goldstein AM, Fraser MC, Struewing JP, Hussussian CJ, Ranade K, Zametkin DP, et al. Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations. N Engl J Med 1995;333:970-1
-
(1995)
N Engl J Med
, vol.333
, pp. 970-971
-
-
Goldstein, A.M.1
Fraser, M.C.2
Struewing, J.P.3
Hussussian, C.J.4
Ranade, K.5
Zametkin, D.P.6
-
29
-
-
0038819652
-
The INK4a/ARF locus and melanoma
-
Sharpless NE, Chin L. The INK4a/ARF locus and melanoma. Oncogene 2003;22:3092-8
-
(2003)
Oncogene
, vol.22
, pp. 3092-3098
-
-
Sharpless, N.E.1
Chin, L.2
-
30
-
-
0031963952
-
Novel mutations in the p16/CDKN2A binding region of the cyclin-dependent kinase-4 gene
-
Tsoa H, Benoit E, Sober AJ, Thiele C, Haluska FG. Novel mutations in the p16/CDKN2A binding region of the cyclin-dependent kinase-4 gene. Cancer Res 1998;58:109-13
-
(1998)
Cancer Res
, vol.58
, pp. 109-113
-
-
Tsoa, H.1
Benoit, E.2
Sober, A.J.3
Thiele, C.4
Haluska, F.G.5
-
31
-
-
0031594829
-
Homozygous deletion of the p16INK4a and the p15INK4b tumour suppressor genes in a subset of human sporadic cutaneous malignant melanoma
-
Wagner SN, Wagner C, Briedigkeit L, Goos M. Homozygous deletion of the p16INK4a and the p15INK4b tumour suppressor genes in a subset of human sporadic cutaneous malignant melanoma. Br J Dermatol 1998;138:13-21
-
(1998)
Br J Dermatol
, vol.138
, pp. 13-21
-
-
Wagner, S.N.1
Wagner, C.2
Briedigkeit, L.3
Goos, M.4
-
32
-
-
0032549704
-
The Ink4a tumor suppressor gene product, p19Arf, interacts with MDM2 and neutralizes MDM2's inhibition of p53
-
Pomerantz J, Schreiber-Agus N, Liegeois NJ, Silverman A, Alland L, Chin L, et al. The Ink4a tumor suppressor gene product, p19Arf, interacts with MDM2 and neutralizes MDM2's inhibition of p53. Cell 1998;92:713-23
-
(1998)
Cell
, vol.92
, pp. 713-723
-
-
Pomerantz, J.1
Schreiber-Agus, N.2
Liegeois, N.J.3
Silverman, A.4
Alland, L.5
Chin, L.6
-
33
-
-
0032493350
-
Functional and physical interactions of the ARF tumor suppressor with p53 and Mdm2
-
Kamijo T, Weber JD, Zambetti G, Zindy F, Roussel MF, Sherr CJ. Functional and physical interactions of the ARF tumor suppressor with p53 and Mdm2. Proc Natl Acad Sci U S A 1998;95:8292-7
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 8292-8297
-
-
Kamijo, T.1
Weber, J.D.2
Zambetti, G.3
Zindy, F.4
Roussel, M.F.5
Sherr, C.J.6
-
34
-
-
0032169516
-
The alternative product from the human CDKN2A locus, p14(ARF), participates in a regulatory feedback loop with p53 and MDM2
-
Stott FJ, Bates S, James MC, McConnell BB, Starborg M, Brookes S, et al. The alternative product from the human CDKN2A locus, p14(ARF), participates in a regulatory feedback loop with p53 and MDM2. EMBO J 1998;17:5001-14
-
(1998)
EMBO J
, vol.17
, pp. 5001-5014
-
-
Stott, F.J.1
Bates, S.2
James, M.C.3
McConnell, B.B.4
Starborg, M.5
Brookes, S.6
-
35
-
-
0032549711
-
ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the RB and p53 tumor suppression pathways
-
Zhang Y, Xiong Y, Yarbrough WG. ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the RB and p53 tumor suppression pathways. Cell 1998;92:725-34
-
(1998)
Cell
, vol.92
, pp. 725-734
-
-
Zhang, Y.1
Xiong, Y.2
Yarbrough, W.G.3
-
36
-
-
70350152582
-
Genetic risk factors for melanoma
-
Meyle KD, Gulberg P. Genetic risk factors for melanoma. Hum Genet 2009;126:499-510
-
(2009)
Hum Genet
, vol.126
, pp. 499-510
-
-
Meyle, K.D.1
Gulberg, P.2
-
37
-
-
33750567811
-
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL
-
Goldstein AM, Chan M, Harland M, Gillanders EM, Hayward NK, Avril MF, et al. High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL. Cancer Res 2006;66:9818-28
-
(2006)
Cancer Res
, vol.66
, pp. 9818-9828
-
-
Goldstein, A.M.1
Chan, M.2
Harland, M.3
Gillanders, E.M.4
Hayward, N.K.5
Avril, M.F.6
-
38
-
-
38049021654
-
Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas
-
Helsing P, Nymoen DA, Ariansen S, Steine SJ, Maehle L, Aamdal S, et al. Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas. Genes Chromosomes Cancer 2008;47:175-84
-
(2008)
Genes Chromosomes Cancer
, vol.47
, pp. 175-184
-
-
Helsing, P.1
Nymoen, D.A.2
Ariansen, S.3
Steine, S.J.4
Maehle, L.5
Aamdal, S.6
-
39
-
-
23044505848
-
A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutations
-
Molven A, Grimstvedt MB, Steine SJ, Harland M, Avril MF, Hayward NK, et al. A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutations. Genes Chromosomes Cancer 2005;44:10-8
-
(2005)
Genes Chromosomes Cancer
, vol.44
, pp. 10-18
-
-
Molven, A.1
Grimstvedt, M.B.2
Steine, S.J.3
Harland, M.4
Avril, M.F.5
Hayward, N.K.6
-
40
-
-
65449116099
-
Identification of a CDK4 R24H mutation-positive melanoma family by analysis of early-onset melanoma patients in Latvia
-
Pjanova D, Molven A, Akslen LA, Engele L, Streinerte B, Azarjana K, et al. Identification of a CDK4 R24H mutation-positive melanoma family by analysis of early-onset melanoma patients in Latvia. Melanoma Res 2009;19:119-22
-
(2009)
Melanoma Res
, vol.19
, pp. 119-122
-
-
Pjanova, D.1
Molven, A.2
Akslen, L.A.3
Engele, L.4
Streinerte, B.5
Azarjana, K.6
-
41
-
-
1242307966
-
Interactive effects of MC1R and OCA2 on melanoma risk phenotypes
-
Duffy DL, Box NF, Chen W, Palmer JS, Montgomery GW, James MR, et al. Interactive effects of MC1R and OCA2 on melanoma risk phenotypes. Hum Mol Genet 2004;13:447-61
-
(2004)
Hum Mol Genet
, vol.13
, pp. 447-461
-
-
Duffy, D.L.1
Box, N.F.2
Chen, W.3
Palmer, J.S.4
Montgomery, G.W.5
James, M.R.6
-
42
-
-
0034127724
-
Cyclic AMP. A key messenger in the regulation of skin pigmentation
-
Busca R, Ballotti R, Cyclic AMP. a key messenger in the regulation of skin pigmentation. Pigment Cell Res 2000;13: 60-9
-
(2000)
Pigment Cell Res
, vol.13
, pp. 60-69
-
-
Busca, R.1
Ballotti, R.2
-
43
-
-
0029839525
-
The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma
-
Valverde P, Healy E, Sikkink S, Haldane F, Thody AJ, Carothers A, et al. The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma. Hum Mol Genet 1996;5: 1663-6
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1663-1666
-
-
Valverde, P.1
Healy, E.2
Sikkink, S.3
Haldane, F.4
Thody, A.J.5
Carothers, A.6
-
44
-
-
0027413475
-
Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function
-
Robbins LS, Nadeau JH, Johnson KR, Kelly MA, Roselli-Rehfuss L, Baack E, et al. Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function. Cell 1993;72:827-34
-
(1993)
Cell
, vol.72
, pp. 827-834
-
-
Robbins, L.S.1
Nadeau, J.H.2
Johnson, K.R.3
Kelly, M.A.4
Roselli-Rehfuss, L.5
Baack, E.6
-
45
-
-
0028580515
-
Molecular and developmental genetics of mouse coat color
-
Jackson IJ. Molecular and developmental genetics of mouse coat color. Ann Rev Genet 1994;28:189-217
-
(1994)
Ann Rev Genet
, vol.28
, pp. 189-217
-
-
Jackson, I.J.1
-
46
-
-
0037902558
-
The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes
-
Sturm RA, Duffy DL, Box NF, Chen W, Smit DJ, Brown DL, et al. The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes. Pigment Cell Res 2003;16:266-72
-
(2003)
Pigment Cell Res
, vol.16
, pp. 266-272
-
-
Sturm, R.A.1
Duffy, D.L.2
Box, N.F.3
Chen, W.4
Smit, D.J.5
Brown, D.L.6
-
47
-
-
0008382604
-
Participation of the melanocortin-1 receptor in the UV control of pigmentation
-
Suzuki I, Im S, Tada A, Scott C, Akcali C, Davis MB, et al. Participation of the melanocortin-1 receptor in the UV control of pigmentation. J Investig Dermatol Symp Proc 1999;4:29-34
-
(1999)
J Investig Dermatol Symp Proc
, vol.4
, pp. 29-34
-
-
Suzuki, I.1
Im, S.2
Tada, A.3
Scott, C.4
Akcali, C.5
Davis, M.B.6
-
48
-
-
0035904403
-
Human pigmentation genes: Identification, structure and consequences of polymorphic variation
-
Sturm RA, Teasdale RD, Box NF. Human pigmentation genes: Identification, structure and consequences of polymorphic variation. Gene 2001;277:49-62
-
(2001)
Gene
, vol.277
, pp. 49-62
-
-
Sturm, R.A.1
Teasdale, R.D.2
Box, N.F.3
-
50
-
-
0344603629
-
Loss of function mutations of the human melanocortin 1 receptor are common and are associated with red hair
-
Schioth HB, Sr Phillips, Rudzish R, Birch-Machin MA, Wikberg JE, Rees JL. Loss of function mutations of the human melanocortin 1 receptor are common and are associated with red hair. Biochem Biophys Res Commun 1999;260:488-91
-
(1999)
Biochem Biophys Res Commun
, vol.260
, pp. 488-491
-
-
Schioth, H.B.1
Phillips Rudzish, R.2
Birch-Machin, M.A.3
Wikberg, J.E.4
Rees, J.L.5
-
51
-
-
0025779123
-
Pheomelanin as well as eumelanin is present in human epidermis
-
Thody AJ, Higgins EM, Wakamatsu K, Ito S, Burchill SA, Marks JM. Pheomelanin as well as eumelanin is present in human epidermis. J Invest Dermatol 1991;97:340-4
-
(1991)
J Invest Dermatol
, vol.97
, pp. 340-344
-
-
Thody, A.J.1
Higgins, E.M.2
Wakamatsu, K.3
Ito, S.4
Burchill, S.A.5
Marks, J.M.6
-
52
-
-
0343694411
-
Microanalysis of melanins in mammalian hair by alkaline hydrogen peroxide degradation: Identification of a new structural marker of pheomelanins
-
Napolitano A, Vincensi MR, Di Donato P, Monfrecola G, Prota G. Microanalysis of melanins in mammalian hair by alkaline hydrogen peroxide degradation: Identification of a new structural marker of pheomelanins. J Invest Dermatol 2000; 114:1141-7
-
(2000)
J Invest Dermatol
, vol.114
, pp. 1141-1147
-
-
Napolitano, A.1
Vincensi, M.R.2
Di Donato, P.3
Monfrecola, G.4
Prota, G.5
-
53
-
-
77953596353
-
Protection against UVR involves MC1R-mediated non-pigmentary and pigmentary mechanisms in vivo
-
Robinson S, Dixon S, Augus S, Diffey B, Wakamatsu K, Ito S, et al. Protection against UVR involves MC1R-mediated non-pigmentary and pigmentary mechanisms in vivo. J Invest Dermatol 2010;130:1904-13
-
(2010)
J Invest Dermatol
, vol.130
, pp. 1904-1913
-
-
Robinson, S.1
Dixon, S.2
Augus, S.3
Diffey, B.4
Wakamatsu, K.5
Ito, S.6
-
54
-
-
0028786945
-
Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans
-
Valverde P, Healy E, Jackson I, Rees JL, Thody AJ. Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans. Nat Genet 1995;11:328-30
-
(1995)
Nat Genet
, vol.11
, pp. 328-330
-
-
Valverde, P.1
Healy, E.2
Jackson, I.3
Rees, J.L.4
Thody, A.J.5
-
55
-
-
43049148341
-
MC1R variants, melanoma and red hair color phenotype: A meta-analysis
-
Raimondi S, Sera F, Gandini S, Iodice S, Caini S, Maisonneuve P, et al. MC1R variants, melanoma and red hair color phenotype: A meta-analysis. Int J Cancer 2008;122:2753-60
-
(2008)
Int J Cancer
, vol.122
, pp. 2753-2760
-
-
Raimondi, S.1
Sera, F.2
Gandini, S.3
Iodice, S.4
Caini, S.5
Maisonneuve, P.6
-
56
-
-
67649365613
-
MC1R variant alleles and malignant melanoma risk in Israel
-
Galore-Haskel G, Azizi E, Mohamdi H, Scope A, Chaudru V, Laitman Y, et al. MC1R variant alleles and malignant melanoma risk in Israel. Eur J Cancer 2009;45:2015-22
-
(2009)
Eur J Cancer
, vol.45
, pp. 2015-2022
-
-
Galore-Haskel, G.1
Azizi, E.2
Mohamdi, H.3
Scope, A.4
Chaudru, V.5
Laitman, Y.6
-
57
-
-
0033910271
-
Melanocortin-1 receptor polymorphisms and risk of melanoma is the association explained solely by pigmentation phenotype?
-
Palmer JS, Duffy DL, Box NF, Aitken JF, O'Gorman LE, Green AC, et al. Melanocortin-1 receptor polymorphisms and risk of melanoma: Is the association explained solely by pigmentation phenotype? Am J Hum Genet 2000;66:176-86
-
(2000)
Am J Hum Genet
, vol.66
, pp. 176-186
-
-
Palmer, J.S.1
Duffy, D.L.2
Box, N.F.3
Aitken, J.F.4
O'Gorman, L.E.5
Green, A.C.6
-
58
-
-
33845496518
-
Variations of the melanocortin-1 receptor and the glutathione-S transferase T1 and M1 genes in cutaneous malignant melanoma
-
Mössner R, Anders N, König I, Krüger U, Schmidt D, Berking C, et al. Variations of the melanocortin-1 receptor and the glutathione-S transferase T1 and M1 genes in cutaneous malignant melanoma. Arch Dermatol Res 2007;298:371-9
-
(2007)
Arch Dermatol Res
, vol.298
, pp. 371-379
-
-
Mössner, R.1
Anders, N.2
König, I.3
Krüger, U.4
Schmidt, D.5
Berking, C.6
-
59
-
-
80051959840
-
Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma
-
Chatzinasiou F, Lill CM, Kypreou K, Stefanaki I, Nicolaou V, Spyrou G, et al. Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma. J Natl Cancer Inst 2011;103:1227-35
-
(2011)
J Natl Cancer Inst
, vol.103
, pp. 1227-1235
-
-
Chatzinasiou, F.1
Lill, C.M.2
Kypreou, K.3
Stefanaki, I.4
Nicolaou, V.5
Spyrou, G.6
-
60
-
-
0034837773
-
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
-
Box NF, Duffy DL, Chen W, Stark M, Martin NG, Sturm RA, et al. MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations. Am J Hum Genet 2001;69: 765-73
-
(2001)
Am J Hum Genet
, vol.69
, pp. 765-773
-
-
Box, N.F.1
Duffy, D.L.2
Chen, W.3
Stark, M.4
Martin, N.G.5
Sturm, R.A.6
-
61
-
-
0034834961
-
Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma
-
van der Velden PA, Sandkuijl LA, Bergman W, Pavel S, van Mourik L, Frants RR, et al. Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma. Am J Hum Genet 2001;69:774-9
-
(2001)
Am J Hum Genet
, vol.69
, pp. 774-779
-
-
Van Der Velden, P.A.1
Sandkuijl, L.A.2
Bergman, W.3
Pavel, S.4
Van Mourik, L.5
Frants, R.R.6
-
62
-
-
66949130735
-
Pigmentation-related genes and their implication in malignant melanoma susceptibility
-
Fernandez LP, Milne RL, Pita G, Floristan U, Sendagorta E, Feito M, et al. Pigmentation-related genes and their implication in malignant melanoma susceptibility. Exp Dermatol 2009;18:634-42
-
(2009)
Exp Dermatol
, vol.18
, pp. 634-642
-
-
Fernandez, L.P.1
Milne, R.L.2
Pita, G.3
Floristan, U.4
Sendagorta, E.5
Feito, M.6
-
63
-
-
45549097424
-
ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma
-
Gudbjartsson DF, Sulem P, Stacey SN, Goldstein AM, Rafnar T, Sigurgeirsson B, et al. ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma. Nat Genet 2008;48:886-91
-
(2008)
Nat Genet
, vol.48
, pp. 886-891
-
-
Gudbjartsson, D.F.1
Sulem, P.2
Stacey, S.N.3
Goldstein, A.M.4
Rafnar, T.5
Sigurgeirsson, B.6
-
64
-
-
45549095745
-
Two newly identified genetic determinants of pigmentation in Europeans
-
Sulem P, Gudbjartsson DF, Stacey SN, Helgason A, Rafnar T, Jakobsdottir M, et al. Two newly identified genetic determinants of pigmentation in Europeans. Nat Genet 2008;40: 835-7
-
(2008)
Nat Genet
, vol.40
, pp. 835-837
-
-
Sulem, P.1
Gudbjartsson, D.F.2
Stacey, S.N.3
Helgason, A.4
Rafnar, T.5
Jakobsdottir, M.6
-
65
-
-
67650073375
-
Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians
-
Nan H, Kraft P, Hunter DJ, Han J. Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians. Int J Cancer 2009;125:909-17
-
(2009)
Int J Cancer
, vol.125
, pp. 909-917
-
-
Nan, H.1
Kraft, P.2
Hunter, D.J.3
Han, J.4
-
66
-
-
45549095449
-
Common sequence variants on 20q11.22 confer melanoma susceptibility
-
Brown KM, Macgregor S, Montgomery GW, Craig DW, Zhao ZZ, Iyadurai K, et al. Common sequence variants on 20q11.22 confer melanoma susceptibility. Nat Genet 2008;40:838-40
-
(2008)
Nat Genet
, vol.40
, pp. 838-840
-
-
Brown, K.M.1
Macgregor, S.2
Montgomery, G.W.3
Craig, D.W.4
Zhao, Z.Z.5
Iyadurai, K.6
-
67
-
-
0036181358
-
A polymorphism in the agouti signaling protein gene is associated with human pigmentation
-
Kanetsky PA, Swoyer J, Panossian S, Holmes R, Guerry D, Rebbeck TR. A polymorphism in the agouti signaling protein gene is associated with human pigmentation. Am J Hum Genet 2002;70:770-5
-
(2002)
Am J Hum Genet
, vol.70
, pp. 770-775
-
-
Kanetsky, P.A.1
Swoyer, J.2
Panossian, S.3
Holmes, R.4
Guerry, D.5
Rebbeck, T.R.6
-
68
-
-
0034697167
-
A common temperature-sensitive allelic form of human tyrosinase is retained in the endoplasmic reticulum at the nonpermissive temperature
-
Berson JF, Frank DW, Calvo PA, Bieler BM, Marks MS. A common temperature-sensitive allelic form of human tyrosinase is retained in the endoplasmic reticulum at the nonpermissive temperature. J Biol Chem 2000;275:12281-9
-
(2000)
J Biol Chem
, vol.275
, pp. 12281-12289
-
-
Berson, J.F.1
Frank, D.W.2
Calvo, P.A.3
Bieler, B.M.4
Marks, M.S.5
-
69
-
-
23644448602
-
Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma
-
Jannot AS, Meziani R, Bertrand G, Gérard B, Descamps V, Archimbaud A, et al. Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma. Eur J Hum Genet 2005;13:913-20
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 913-920
-
-
Jannot, A.S.1
Meziani, R.2
Bertrand, G.3
Gérard, B.4
Descamps, V.5
Archimbaud, A.6
-
70
-
-
51549094379
-
SLC45A2: A novel malignant melanoma-associated gene
-
Fernandez LP, Milne RL, Pita G, Avilés JA, Lázaro P, Benítez J, et al. SLC45A2: A novel malignant melanoma-associated gene. Hum Mutat 2008;29:1161-7
-
(2008)
Hum Mutat
, vol.29
, pp. 1161-1167
-
-
Fernandez, L.P.1
Milne, R.L.2
Pita, G.3
Avilés, J.A.4
Lázaro, P.5
Benítez, J.6
-
71
-
-
51549103690
-
Variants of the MATP/SLC45A2 gene are protective for melanoma in the French population
-
Guedj M, Bourillon A, Combadiéres C, Rodero M, Dieudé P, Descamps V, et al. Variants of the MATP/SLC45A2 gene are protective for melanoma in the French population. Hum Mutat 2008;29:1154-60
-
(2008)
Hum Mutat
, vol.29
, pp. 1154-1160
-
-
Guedj, M.1
Bourillon, A.2
Combadiéres, C.3
Rodero, M.4
Dieudé, P.5
Descamps, V.6
-
72
-
-
75549084094
-
Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma
-
Duffy DL, Zhao ZZ, Sturm RA, Hayward NK, Martin NG, Montgomery GW. Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma. J Invest Dermatol 2010; 130:520-8
-
(2010)
J Invest Dermatol
, vol.130
, pp. 520-528
-
-
Duffy, D.L.1
Zhao, Z.Z.2
Sturm, R.A.3
Hayward, N.K.4
Martin, N.G.5
Montgomery, G.W.6
-
73
-
-
0035144754
-
Childhood sun exposure as a risk factor for melanoma: A systematic review of epidemiological studies
-
Whiteman DC, Whiteman CA, Green AC. Childhood sun exposure as a risk factor for melanoma: A systematic review of epidemiological studies. Cancer Causes Control 2001;12: 69-82
-
(2001)
Cancer Causes Control
, vol.12
, pp. 69-82
-
-
Whiteman, D.C.1
Whiteman, C.A.2
Green, A.C.3
-
74
-
-
0021940118
-
High risk of malignant melanoma in melanoma-prone families with dysplastic nevi
-
Greene MH, Clark WH Jr, Tucker MA, Kraemer KH, Elder DE, Fraser MC. High risk of malignant melanoma in melanoma-prone families with dysplastic nevi. Ann Intern Med 1985;102:458-65
-
(1985)
Ann Intern Med
, vol.102
, pp. 458-465
-
-
Greene, M.H.1
Clark, Jr.W.H.2
Tucker, M.A.3
Kraemer, K.H.4
Elder, D.E.5
Fraser, M.C.6
-
75
-
-
68149100807
-
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi
-
Falchi M, Bataille V, Hayward NK, Duffy DL, Bishop JA, Pastinen T, et al. Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. Nat Genet 2009;41:915-9
-
(2009)
Nat Genet
, vol.41
, pp. 915-919
-
-
Falchi, M.1
Bataille, V.2
Hayward, N.K.3
Duffy, D.L.4
Bishop, J.A.5
Pastinen, T.6
-
76
-
-
79958759586
-
Genome-wide associated study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk
-
Nan H, Xu M, Zhang J, Zhang M, Kraft P, Qureshi AA, et al. Genome-wide associated study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk.Hum Mol Genet 2011;20:2673-9
-
(2011)
Hum Mol Genet
, vol.20
, pp. 2673-2679
-
-
Nan, H.1
Xu, M.2
Zhang, J.3
Zhang, M.4
Kraft, P.5
Qureshi, A.A.6
-
77
-
-
44849091227
-
A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation
-
Han J, Kraft P, Nan H, Guo Q, Chen C, Qureshi A, et al. A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. PLoS Genet 2008;4:1-11
-
(2008)
PLoS Genet
, vol.4
, pp. 1-11
-
-
Han, J.1
Kraft, P.2
Nan, H.3
Guo, Q.4
Chen, C.5
Qureshi, A.6
-
78
-
-
36549071998
-
Genetic determinants of hair, eye and skin pigmentation in Europeans
-
Sulem P, Gudbjartsson DF, Stacey S, Helgason A, Rafnar T, Magnusson KP, et al. Genetic determinants of hair, eye and skin pigmentation in Europeans. Nat Genet 2007;39:1443-52
-
(2007)
Nat Genet
, vol.39
, pp. 1443-1452
-
-
Sulem, P.1
Gudbjartsson, D.F.2
Stacey, S.3
Helgason, A.4
Rafnar, T.5
Magnusson, K.P.6
-
79
-
-
65149096689
-
Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation
-
Wang ZQ, Si L, Tang Q, Lin D, Fu Z, Zhang J, et al. Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation. Am J Hum Genet 2009;84:672-7
-
(2009)
Am J Hum Genet
, vol.84
, pp. 672-677
-
-
Wang, Z.Q.1
Si, L.2
Tang, Q.3
Lin, D.4
Fu, Z.5
Zhang, J.6
-
80
-
-
0346880454
-
Cytokine gene single nucleotide polymorphisms and susceptibility to and prognosis in cutaneous malignant melanoma
-
Howell WM, Turner SJ, Theaker JM, Bateman AC. Cytokine gene single nucleotide polymorphisms and susceptibility to and prognosis in cutaneous malignant melanoma. Eur J Immunogenet 2003;30:409-14
-
(2003)
Eur J Immunogenet
, vol.30
, pp. 409-414
-
-
Howell, W.M.1
Turner, S.J.2
Theaker, J.M.3
Bateman, A.C.4
-
81
-
-
0027496921
-
Analysis of antigens recognised on human melanoma cells by A2-restricted cytolytic T lymphocytes (CTL)
-
Wolfel T, Hauer M, Klehmann E, Brichard V, Ackermann B, Knuth A, et al. Analysis of antigens recognised on human melanoma cells by A2-restricted cytolytic T lymphocytes (CTL). Int J Cancer 1993;55:237
-
(1993)
Int J Cancer
, vol.55
, pp. 237
-
-
Wolfel, T.1
Hauer, M.2
Klehmann, E.3
Brichard, V.4
Ackermann, B.5
Knuth, A.6
-
82
-
-
53549134937
-
Interleukin and interleukin receptor gene polymorphisms and susceptibility to melanoma
-
Gu F, Qureshi AA, Niu T, Kraft P, Guo Q, Hunter DJ, et al. Interleukin and interleukin receptor gene polymorphisms and susceptibility to melanoma. Melanoma Res 2008;18: 330-5
-
(2008)
Melanoma Res
, vol.18
, pp. 330-325
-
-
Gu, F.1
Qureshi, A.A.2
Niu, T.3
Kraft, P.4
Guo, Q.5
Hunter, D.J.6
-
83
-
-
0001432368
-
Depressed immunity and skin cancer
-
Penn I. Depressed immunity and skin cancer. Immunol Today 1984;5:291-3
-
(1984)
Immunol Today
, vol.5
, pp. 291-293
-
-
Penn, I.1
-
84
-
-
14844350948
-
Influence of interleukin-10 genetic polymorphism on survival rates in melanoma patients with advanced disease
-
Alonso R, Suarez A, Castro P, Lacave AJ, Gutierrez C. Influence of interleukin-10 genetic polymorphism on survival rates in melanoma patients with advanced disease. Melanoma Res 2005;15:53-60
-
(2005)
Melanoma Res
, vol.15
, pp. 53-60
-
-
Alonso, R.1
Suarez, A.2
Castro, P.3
Lacave, A.J.4
Gutierrez, C.5
-
85
-
-
0031017238
-
An investigation of polymorphisms in the interleukin-10 gene promoter
-
Turner DM, Williams DM, Sankaran D, Lazarus M, Sinnott PJ, Hutchinson IV. An investigation of polymorphisms in the interleukin-10 gene promoter. Eur JImmunogenet 1997;24:1-8
-
(1997)
Eur J Immunogenet
, vol.24
, pp. 1-8
-
-
Turner, D.M.1
Williams, D.M.2
Sankaran, D.3
Lazarus, M.4
Sinnott, P.J.5
Hutchinson, I.V.6
-
86
-
-
0031946335
-
IL-10 gene promoter polymorphisms in rheumatoid arthritis
-
Hajeer AH, Lazarus M, Turner D, Mageed RA, Vencovsky J, Sinnott P, et al. IL-10 gene promoter polymorphisms in rheumatoid arthritis. Scand J Rheumatol 1998;27:142-5
-
(1998)
Scand J Rheumatol
, vol.27
, pp. 142-145
-
-
Hajeer, A.H.1
Lazarus, M.2
Turner, D.3
Mageed, R.A.4
Vencovsky, J.5
Sinnott, P.6
-
87
-
-
0036753243
-
Interleukin-10, interleukin-6 and interferon-gamma gene polymorphisms in melanoma patients
-
Martinez-Escribano JA, Moya-Quiles MR, Muro M, Montes-Ares O, Hernández-Caselles T, Frías JF, et al. Interleukin-10, interleukin-6 and interferon-gamma gene polymorphisms in melanoma patients. Melanoma Res 2002;12:465-9
-
(2002)
Melanoma Res
, vol.12
, pp. 465-469
-
-
Martinez-Escribano, J.A.1
Moya-Quiles, M.R.2
Muro, M.3
Montes-Ares, O.4
Hernández-Caselles, T.5
Frías, J.F.6
-
88
-
-
33845954805
-
Association of cytokine gene polymorphisms with malignant melanoma in Caucasian population
-
Nikolova PN, Pawelec GP, Mihailova SM, Ivanova MI, Myhailova AP, Baltadjieva DN, et al. Association of cytokine gene polymorphisms with malignant melanoma in Caucasian population. Cancer Immunol Immunother 2007;56:371-9
-
(2007)
Cancer Immunol Immunother
, vol.56
, pp. 371-379
-
-
Nikolova, P.N.1
Pawelec, G.P.2
Mihailova, S.M.3
Ivanova, M.I.4
Myhailova, A.P.5
Baltadjieva, D.N.6
-
89
-
-
0028966911
-
Elevated serum levels of interleukin-10 in patients with metastatic malignant melanoma
-
Dummer W, Becker JC, Schwaaf A, Leverkus M, Moll T, Bröcker EB. Elevated serum levels of interleukin-10 in patients with metastatic malignant melanoma. Melanoma Res 1995;5: 67-8
-
(1995)
Melanoma Res
, vol.5
, pp. 67-68
-
-
Dummer, W.1
Becker, J.C.2
Schwaaf, A.3
Leverkus, M.4
Moll, T.5
Bröcker, E.B.6
-
90
-
-
0030950036
-
Interleukin-10 is a growth factor for human melanoma cells and down-regulates HLA class-I, HLA class-II and ICAM-1 molecules
-
Yue FY, Dummer R, Geersten R, Hofbauer G, Laine E, Manolio S, et al. Interleukin-10 is a growth factor for human melanoma cells and down-regulates HLA class-I, HLA class-II and ICAM-1 molecules. Int J Cancer 1997;71:630-7
-
(1997)
Int J Cancer
, vol.71
, pp. 630-637
-
-
Yue, F.Y.1
Dummer, R.2
Geersten, R.3
Hofbauer, G.4
Laine, E.5
Manolio, S.6
-
91
-
-
12944291453
-
Impact of gene polymorphisms on clinical outcome for stage IV melanoma patients treated with biochemotherapy: An exploratory study
-
Liu D, O'Day SJ, Yang D, Boasberg P, Milford R, Kristedja T, et al. Impact of gene polymorphisms on clinical outcome for stage IV melanoma patients treated with biochemotherapy: An exploratory study. Clin Cancer Res 2005;11:1237-46
-
(2005)
Clin Cancer Res
, vol.11
, pp. 1237-1246
-
-
Liu, D.1
O'Day, S.J.2
Yang, D.3
Boasberg, P.4
Milford, R.5
Kristedja, T.6
-
92
-
-
40749136181
-
A phase i clinical study of vaccination of melanoma patients with dendritic cells loaded with allogeneic apoptotic/necrotic melanoma cells. Analysis of toxicity and immune response to the vaccine and of IL-10 -1082 promoter genotype as predictor of disease progression
-
von Euw EM, Barrio MM, Furman D, Levy EM, Bianchini M, Pequillet I, et al. A phase I clinical study of vaccination of melanoma patients with dendritic cells loaded with allogeneic apoptotic/necrotic melanoma cells. Analysis of toxicity and immune response to the vaccine and of IL-10 -1082 promoter genotype as predictor of disease progression. J Transl Med 2008;6:1-14
-
(2008)
J Transl Med
, vol.6
, pp. 1-14
-
-
Von Euw, E.M.1
Barrio, M.M.2
Furman, D.3
Levy, E.M.4
Bianchini, M.5
Pequillet, I.6
-
93
-
-
0035984986
-
Influence of TNFa and LTa single nucleotide polymorphisms on susceptibility to and prognosis in cutaneous malignant melanoma in the British population
-
Howell WM, Turner SJ, Collins A, Bateman AC, Theaker JM. Influence of TNFa and LTa single nucleotide polymorphisms on susceptibility to and prognosis in cutaneous malignant melanoma in the British population. Eur J Immunogenet 2002;29:17-23
-
(2002)
Eur J Immunogenet
, vol.29
, pp. 17-23
-
-
Howell, W.M.1
Turner, S.J.2
Collins, A.3
Bateman, A.C.4
Theaker, J.M.5
-
94
-
-
33644893065
-
HLA class II polymorphisms in Spanish melanoma patients: Homozygosity for HLA-DQA1 locus can be a potential melanoma risk factor
-
Planelles D, Nagore E, Moret A, Botella-Estrada R, Villa E, Guillén C, et al. HLA class II polymorphisms in Spanish melanoma patients: homozygosity for HLA-DQA1 locus can be a potential melanoma risk factor. Br J Dermatol 2006;154: 261-6
-
(2006)
Br J Dermatol
, vol.154
, pp. 261-266
-
-
Planelles, D.1
Nagore, E.2
Moret, A.3
Botella-Estrada, R.4
Villa, E.5
Guillén, C.6
-
95
-
-
0030046190
-
The human leukocyte antigen TAP2 gene defines the centromeric limit of melanoma susceptibility on chromosome 6p
-
Lee JE, Loflin PT, Laud PR, Lu M, Reveille JD, Lawlor DA. The human leukocyte antigen TAP2 gene defines the centromeric limit of melanoma susceptibility on chromosome 6p. Tissue Antigens 1996;47:117-21
-
(1996)
Tissue Antigens
, vol.47
, pp. 117-121
-
-
Lee, J.E.1
Loflin, P.T.2
Laud, P.R.3
Lu, M.4
Reveille, J.D.5
Lawlor, D.A.6
-
97
-
-
0029742870
-
Malignant melanoma: Relationship of the human leukocyte antigen class II gene DQB1.∗0301 to disease recurrence in american joint committee on cancer stage i or II
-
Lee JE, Lu M, Mansfield PF, Platsoucas CD, Reveille JD, Ross MI. Malignant melanoma: Relationship of the human leukocyte antigen class II gene DQB1.∗0301 to disease recurrence in American Joint Committee on Cancer stage I or II. Cancer 1996;78:758-63
-
(1996)
Cancer
, vol.78
, pp. 758-763
-
-
Lee, J.E.1
Lu, M.2
Mansfield, P.F.3
Platsoucas, C.D.4
Reveille, J.D.5
Ross, M.I.6
-
98
-
-
0029549950
-
HLA associations in the antitumor response against malignant melanoma
-
Marincola FM, Shamamian P, Rivoltini L, Salgaller M, Cormier J, Restifo NP, et al. HLA associations in the antitumor response against malignant melanoma. J Immunother 1995;18:242-52
-
(1995)
J Immunother
, vol.18
, pp. 242-252
-
-
Marincola, F.M.1
Shamamian, P.2
Rivoltini, L.3
Salgaller, M.4
Cormier, J.5
Restifo, N.P.6
-
99
-
-
0031757832
-
Molecular analysis of HLA DRB1 and DQB1 polymorphism in Italian melanoma patients
-
Lombardi ML, Mercuro O, Pirozzi G, Ionna F, Lombari V, Mozzillo N, et al. Molecular analysis of HLA DRB1 and DQB1 polymorphism in Italian melanoma patients. J Immunother 1998;21:435-9
-
(1998)
J Immunother
, vol.21
, pp. 435-439
-
-
Lombardi, M.L.1
Mercuro, O.2
Pirozzi, G.3
Ionna, F.4
Lombari, V.5
Mozzillo, N.6
-
100
-
-
6844265573
-
HLA-DR and eDQ alleles in Italian patients with melanoma
-
Lulli P, Grammatico P, Brioli G, Catricalá C, Morellini M, Roccella M, et al. HLA-DR and eDQ alleles in Italian patients with melanoma. Tissue Antigens 1998;51:276-80
-
(1998)
Tissue Antigens
, vol.51
, pp. 276-280
-
-
Lulli, P.1
Grammatico, P.2
Brioli, G.3
Catricalá, C.4
Morellini, M.5
Roccella, M.6
-
101
-
-
8244232507
-
Molecular genetic analysis of HLA class II alleles in Japanese patients with melanoma
-
Kageshita T, Naruse T, Hirai S, Ono T, Horikoshi T, Nakagawa H, et al. Molecular genetic analysis of HLA class II alleles in Japanese patients with melanoma. Tissue Antigens 1997;49: 466-70
-
(1997)
Tissue Antigens
, vol.49
, pp. 466-470
-
-
Kageshita, T.1
Naruse, T.2
Hirai, S.3
Ono, T.4
Horikoshi, T.5
Nakagawa, H.6
-
102
-
-
0031594841
-
HLA-DQB1.∗0303 and .∗0301 alleles influence susceptibility to and prognosis in cutaneous malignant melanoma in the british caucasian population
-
Bateman AC, Turner SJ, Theaker JM, Howell WM. HLA-DQB1.∗0303 and .∗0301 alleles influence susceptibility to and prognosis in cutaneous malignant melanoma in the British Caucasian population. Tissue Antigens 1998;52:67-73
-
(1998)
Tissue Antigens
, vol.52
, pp. 67-73
-
-
Bateman, A.C.1
Turner, S.J.2
Theaker, J.M.3
Howell, W.M.4
-
103
-
-
33645458843
-
High risk of cutaneous melanoma amongst carriers of the intercellular adhesion molecule-1 R241 allele
-
Vinceti M, Pellacani G, Casali B, Malagoli C, Nicoli D, Farnetti E, et al. High risk of cutaneous melanoma amongst carriers of the intercellular adhesion molecule-1 R241 allele. Melanoma Res 2006;16:93-6
-
(2006)
Melanoma Res
, vol.16
, pp. 93-96
-
-
Vinceti, M.1
Pellacani, G.2
Casali, B.3
Malagoli, C.4
Nicoli, D.5
Farnetti, E.6
-
105
-
-
0344406948
-
Intercellular adhesion molecule-1 (ICAM-1) gene polymorphisms in endometriosis
-
Vigano P, Infantino M, Lattuada D, Lauletta R, Ponti E, Somigliana E, et al. Intercellular adhesion molecule-1 (ICAM-1) gene polymorphisms in endometriosis. Mol Hum Reprod 2003;9:47-52
-
(2003)
Mol Hum Reprod
, vol.9
, pp. 47-52
-
-
Vigano, P.1
Infantino, M.2
Lattuada, D.3
Lauletta, R.4
Ponti, E.5
Somigliana, E.6
-
106
-
-
0025759969
-
Binding of the integrin Mac-1 (CD11b/CD18) to the third immunoglobulin-like domain of ICAM-1 (CD54) and its regulation by glycosylation
-
Diamond MS, Staunton DE, Marlin SD, Springer TA. Binding of the integrin Mac-1 (CD11b/CD18) to the third immunoglobulin-like domain of ICAM-1 (CD54) and its regulation by glycosylation. Cell 1991;65:961-71
-
(1991)
Cell
, vol.65
, pp. 961-971
-
-
Diamond, M.S.1
Staunton, D.E.2
Marlin, S.D.3
Springer, T.A.4
-
107
-
-
34447099199
-
DNA repair gene polymorphisms and genetic predisposition to cutaneous melanoma
-
Povey JE, Darakhshan F, Robertson K, Bisset Y, Mekky M, Rees J, et al. DNA repair gene polymorphisms and genetic predisposition to cutaneous melanoma. Carcinogenesis 2007;28:1087-93
-
(2007)
Carcinogenesis
, vol.28
, pp. 1087-1093
-
-
Povey, J.E.1
Darakhshan, F.2
Robertson, K.3
Bisset, Y.4
Mekky, M.5
Rees, J.6
-
108
-
-
77956444537
-
Single-nucleotide polymorphisms in DNA-repair genes and cutaneous melanoma
-
Figl A, Scherer D, Nagore E, Bermejo JL, Botella-Estrada R, Gast A, et al. Single-nucleotide polymorphisms in DNA-repair genes and cutaneous melanoma. Mutat Res 2010;702(1):8-16
-
(2010)
Mutat Res
, vol.702
, Issue.1
, pp. 8-16
-
-
Figl, A.1
Scherer, D.2
Nagore, E.3
Bermejo, J.L.4
Botella-Estrada, R.5
Gast, A.6
-
109
-
-
67649976891
-
Polymorphisms in genes involved in DNA repair, cell growth, oxidative stress, and inflammatory response and melanoma risk
-
Gu F, Qureshi AA, Kraft P, Guo Q, Hunter DJ, Han J. Polymorphisms in genes involved in DNA repair, cell growth, oxidative stress, and inflammatory response and melanoma risk. Br J Dermatol 2009;161:209-12
-
(2009)
Br J Dermatol
, vol.161
, pp. 209-212
-
-
Gu, F.1
Qureshi, A.A.2
Kraft, P.3
Guo, Q.4
Hunter, D.J.5
Han, J.6
-
110
-
-
58549098021
-
Single nucleotide polymorphisms in DNA repair genes XRCC1 and APEX1 in progression and survival of primary cutaneous melanoma patients
-
Figl A, Scherer D, Nagore E, Bermejo JL, Dickes E, Thirumaran RK, et al. Single nucleotide polymorphisms in DNA repair genes XRCC1 and APEX1 in progression and survival of primary cutaneous melanoma patients. Mutat Res 2009;661: 78-84
-
(2009)
Mutat Res
, vol.661
, pp. 78-84
-
-
Figl, A.1
Scherer, D.2
Nagore, E.3
Bermejo, J.L.4
Dickes, E.5
Thirumaran, R.K.6
-
111
-
-
65249160573
-
Association of MDM2 SNP309, age of onset, and gender in cutaneous melanoma
-
Firoz EF, Warycha M, Zakrzewski J, Pollens D, Wang G, Shapiro R, et al. Association of MDM2 SNP309, age of onset, and gender in cutaneous melanoma. Clin Cancer Res 2009; 15:2573-80
-
(2009)
Clin Cancer Res
, vol.15
, pp. 2573-2580
-
-
Firoz, E.F.1
Warycha, M.2
Zakrzewski, J.3
Pollens, D.4
Wang, G.5
Shapiro, R.6
-
112
-
-
59449090970
-
Absence of founder BRCA1 and BRCA2 mutations in cutaneous malignant melanoma patients of Ashkenazi origin
-
Kadouri L, Temper M, Grenader T, Abeliovich D, Hamburger T, Peretz T, et al. Absence of founder BRCA1 and BRCA2 mutations in cutaneous malignant melanoma patients of Ashkenazi origin. Fam Cancer 2009;8:29-32
-
(2009)
Fam Cancer
, vol.8
, pp. 29-32
-
-
Kadouri, L.1
Temper, M.2
Grenader, T.3
Abeliovich, D.4
Hamburger, T.5
Peretz, T.6
-
113
-
-
33747877809
-
Genetic variants of the ADPRT, XRCC1 and APE1 genes and risk of cutaneous melanoma
-
Li C, Liu Z, Wang LE, Strom SS, Lee JE, Gershenwald JE, et al. Genetic variants of the ADPRT, XRCC1 and APE1 genes and risk of cutaneous melanoma. Carcinogenesis 2006;27: 1894-901
-
(2006)
Carcinogenesis
, vol.27
, pp. 1894-1901
-
-
Li, C.1
Liu, Z.2
Wang, L.E.3
Strom, S.S.4
Lee, J.E.5
Gershenwald, J.E.6
-
114
-
-
33845988014
-
Polymorphisms in the DNA repair genes XPC, XPD, and XPG and risk of cutaneous melanoma: A case-control analysis
-
Li C, Hu Z, Liu Z, Strom SS, Gershenwald JE, Lee JE, et al. Polymorphisms in the DNA repair genes XPC, XPD, and XPG and risk of cutaneous melanoma: A case-control analysis. Cancer Epidemiol Biomarkers Prev 2006;15:2526-32
-
(2006)
Cancer Epidemiol Biomarkers Prev
, vol.15
, pp. 2526-2532
-
-
Li, C.1
Hu, Z.2
Liu, Z.3
Strom, S.S.4
Gershenwald, J.E.5
Lee, J.E.6
-
115
-
-
79953733129
-
Genetic variants in telomere-maintaining genes and skin cancer risk
-
Nan H, Qureshi AA, Prescott J, De Vivo I, Han J. Genetic variants in telomere-maintaining genes and skin cancer risk. Hum Genet 2011;129:247-53
-
(2011)
Hum Genet
, vol.129
, pp. 247-253
-
-
Nan, H.1
Qureshi, A.A.2
Prescott, J.3
De Vivo, I.4
Han, J.5
-
116
-
-
0026776502
-
Relationship between the debrisoquine hydroxylase polymorphism and cancer susceptibility
-
Wolf CR, Smith CA, Gough AC, Moss JE, Vallis KA, Howard G, et al. Relationship between the debrisoquine hydroxylase polymorphism and cancer susceptibility. Carcinogenesis 1992;13:1035-8
-
(1992)
Carcinogenesis
, vol.13
, pp. 1035-1038
-
-
Wolf, C.R.1
Smith, C.A.2
Gough, A.C.3
Moss, J.E.4
Vallis, K.A.5
Howard, G.6
-
117
-
-
0028829818
-
Human CYP2D6 gene polymorphism in Slovene cancer patients and healthy controls
-
Dolzan V, Rudolf Z, Breskvar K. Human CYP2D6 gene polymorphism in Slovene cancer patients and healthy controls. Carcinogenesis 1995;16:2675-8
-
(1995)
Carcinogenesis
, vol.16
, pp. 2675-2678
-
-
Dolzan, V.1
Rudolf, Z.2
Breskvar, K.3
-
118
-
-
0032767989
-
Cytochrome P450 CYP2D6 genotypes: Association with hair colour, Breslow thickness and melanocyte stimulating hormone receptor alleles in patients with malignant melanoma
-
Strange RC, Ellison T, Ichii-Jones F, Bath J, Hoban P, Lear JT, et al. Cytochrome P450 CYP2D6 genotypes: Association with hair colour, Breslow thickness and melanocyte stimulating hormone receptor alleles in patients with malignant melanoma. Pharmacogenetics 1999;9:269-76
-
(1999)
Pharmacogenetics
, vol.9
, pp. 269-276
-
-
Strange, R.C.1
Ellison, T.2
Ichii-Jones, F.3
Bath, J.4
Hoban, P.5
Lear, J.T.6
-
119
-
-
2942598063
-
Cytochrome P450 gene polymorphism and cancer
-
Agńdez J. Cytochrome P450 gene polymorphism and cancer. Current Drug Metab 2004;5:211-24
-
(2004)
Current Drug Metab
, vol.5
, pp. 211-224
-
-
Agúndez, J.1
-
120
-
-
34249937356
-
Significance of glutathione S-transferases M1, T1, and P1 polymorphisms in Swedish melanoma patients
-
Bu H, Rosdahl I, Holmdahl-Källen K, Sun XF, Zhang H. Significance of glutathione S-transferases M1, T1, and P1 polymorphisms in Swedish melanoma patients. Oncol Rep 2007;17:859-64
-
(2007)
Oncol Rep
, vol.17
, pp. 859-864
-
-
Bu, H.1
Rosdahl, I.2
Holmdahl-Källen, K.3
Sun, X.F.4
Zhang, H.5
-
121
-
-
0035203785
-
Altered glutathione antioxidant metabolism during tumor progression in human renal-cell carcinoma
-
Lusini L, Tripodi SA, Rossi R, Giannerini F, Giustarini D, del Vecchio MT, et al. Altered glutathione antioxidant metabolism during tumor progression in human renal-cell carcinoma. Int J Cancer 2001;91:55-9
-
(2001)
Int J Cancer
, vol.91
, pp. 55-59
-
-
Lusini, L.1
Tripodi, S.A.2
Rossi, R.3
Giannerini, F.4
Giustarini, D.5
Del Vecchio, M.T.6
-
122
-
-
0018896707
-
The glutathione S-transferases: Their role in detoxification and toxification of xenobiotics
-
Baars AJ, Breimer DD. The glutathione S-transferases: Their role in detoxification and toxification of xenobiotics. Ann Biol Clin 1980;38:49-56
-
(1980)
Ann Biol Clin
, vol.38
, pp. 49-56
-
-
Baars, A.J.1
Breimer, D.D.2
-
123
-
-
0030858074
-
Molecular epidemiology of the human glutathione S-transferase genotypes GSTM1 and GSTT1 in cancer susceptibility
-
Rebbeck TR. Molecular epidemiology of the human glutathione S-transferase genotypes GSTM1 and GSTT1 in cancer susceptibility. Cancer Epidemiol Biomarkers Prev 1997;6: 733-74
-
(1997)
Cancer Epidemiol Biomarkers Prev
, vol.6
, pp. 733-774
-
-
Rebbeck, T.R.1
-
124
-
-
0034915417
-
Interaction of glutathione S-transferase M1 and T1 genotypes and malignant melanoma
-
Kanetsky PA, Holmes R, Walker A, Najarian D, Swoyer J, Guerry D, et al. Interaction of glutathione S-transferase M1 and T1 genotypes and malignant melanoma. Cancer Epidemiol Biomarkers Prev 2001;10:509-13
-
(2001)
Cancer Epidemiol Biomarkers Prev
, vol.10
, pp. 509-513
-
-
Kanetsky, P.A.1
Holmes, R.2
Walker, A.3
Najarian, D.4
Swoyer, J.5
Guerry, D.6
-
125
-
-
33745995752
-
Genetic susceptibility to environmental carcinogenesis in Slovenian melanoma patients
-
Dolzan V, Rudolf Z, Breskvar K. Genetic susceptibility to environmental carcinogenesis in Slovenian melanoma patients. Acta Dermatovenerol Alp Panonica Adriat 2006;15:69-78
-
(2006)
Acta Dermatovenerol Alp Panonica Adriat
, vol.15
, pp. 69-78
-
-
Dolzan, V.1
Rudolf, Z.2
Breskvar, K.3
-
126
-
-
33846245970
-
Association between cutaneous melanoma, Breslow thickness and vitamin D receptor BsmI polymorphism
-
Santonocito C, Capizzi R, Concolino MM, Lavieri MM, Paradisi A, Gentileschi S, et al. Association between cutaneous melanoma, Breslow thickness and vitamin D receptor BsmI polymorphism. Br J Dermatol 2007;156:277-82
-
(2007)
Br J Dermatol
, vol.156
, pp. 277-282
-
-
Santonocito, C.1
Capizzi, R.2
Concolino, M.M.3
Lavieri, M.M.4
Paradisi, A.5
Gentileschi, S.6
-
127
-
-
3042687353
-
Differential biological effects of 1,25-dihydroxyvitamin D3 on melanoma cell lines in vitro
-
375-379
-
Seifert M, Rech M, Meineke V, Tilgen W, Reichrath J. Differential biological effects of 1,25-dihydroxyvitamin D3 on melanoma cell lines in vitro. J Steroid Biochem Mol Biol 2004;89-90:375-9
-
(2004)
J Steroid Biochem Mol Biol
, pp. 89-90
-
-
Seifert, M.1
Rech, M.2
Meineke, V.3
Tilgen, W.4
Reichrath, J.5
-
128
-
-
13244284575
-
Vitamin D intake: A global perspective of current status
-
Calvo MS, Whiting SJ, Barton CN. Vitamin D intake: A global perspective of current status. J Nutr 2005;135:310-6
-
(2005)
J Nutr
, vol.135
, pp. 310-316
-
-
Calvo, M.S.1
Whiting, S.J.2
Barton, C.N.3
-
129
-
-
67650155213
-
Review and meta-analysis on vitamin D receptor polymorphisms and cancer risk
-
Raimondi S, Johansson H, Maisonneuve P, Gandini S. Review and meta-analysis on vitamin D receptor polymorphisms and cancer risk. Carcinogenesis 2009;30:1170-80
-
(2009)
Carcinogenesis
, vol.30
, pp. 1170-1180
-
-
Raimondi, S.1
Johansson, H.2
Maisonneuve, P.3
Gandini, S.4
-
130
-
-
0005374834
-
Cloning and expression of full-length cDNA encoding human vitamin D receptor
-
Baker AR, McDonnell DP, Hughes M, Crisp TM, Mangelsdorf DJ, Haussler MR, et al. Cloning and expression of full-length cDNA encoding human vitamin D receptor. Proc Natl Acad Sci U S A 1988;85:3294-8
-
(1988)
Proc Natl Acad Sci U S A
, vol.85
, pp. 3294-3298
-
-
Baker, A.R.1
McDonnell, D.P.2
Hughes, M.3
Crisp, T.M.4
Mangelsdorf, D.J.5
Haussler, M.R.6
-
131
-
-
33846206885
-
Genetic variants of the vitamin D receptor gene alter risk of cutaneous melanoma
-
Li C, Liu Z, Zhang Z, Strom SS, Gershenwald JE, Prieto VG, et al. Genetic variants of the vitamin D receptor gene alter risk of cutaneous melanoma. J Invest Dermatol 2007;127: 276-80
-
(2007)
J Invest Dermatol
, vol.127
, pp. 276-280
-
-
Li, C.1
Liu, Z.2
Zhang, Z.3
Strom, S.S.4
Gershenwald, J.E.5
Prieto, V.G.6
-
132
-
-
79951807758
-
The unfavorable effect of the A allele of the vitamin D receptor promoter polymorphism A-1012G has different mechanisms related to susceptibility and outcome of malignant melanoma
-
Halsall JA, Osborne JE, Epstein MP, Pringle JH, Hutchinson PE. The unfavorable effect of the A allele of the vitamin D receptor promoter polymorphism A-1012G has different mechanisms related to susceptibility and outcome of malignant melanoma. Dermatoendocrinol 2009;1:54-7
-
(2009)
Dermatoendocrinol
, vol.1
, pp. 54-57
-
-
Halsall, J.A.1
Osborne, J.E.2
Epstein, M.P.3
Pringle, J.H.4
Hutchinson, P.E.5
-
133
-
-
40749087320
-
Haplotype and genotypes of the VDR gene and cutaneous melanoma risk in non-Hispanic whites in Texas: A case-control study
-
Li C, Liu Z, Wang LE, Gershenwald JE, Lee JE, Prieto VG, et al. Haplotype and genotypes of the VDR gene and cutaneous melanoma risk in non-Hispanic whites in Texas: A case-control study. Int J Cancer 2008;122:2077-84
-
(2008)
Int J Cancer
, vol.122
, pp. 2077-2084
-
-
Li, C.1
Liu, Z.2
Wang, L.E.3
Gershenwald, J.E.4
Lee, J.E.5
Prieto, V.G.6
-
134
-
-
60149103623
-
Vitamin D and skin cancer: A meta-analysis
-
Gandini S, Raimondi S, Gnagnarella P, Doré JF, Maisonneuve P, Testori A. Vitamin D and skin cancer: A meta-analysis. Eur J Cancer 2009;45:634-41
-
(2009)
Eur J Cancer
, vol.45
, pp. 634-641
-
-
Gandini, S.1
Raimondi, S.2
Gnagnarella, P.3
Doré, J.F.4
Maisonneuve, P.5
Testori, A.6
-
135
-
-
73949092448
-
Serum 25-hydroxyvitamin D3 levels are associated with Breslow thickness at presentation and survival from melanoma
-
Newton-Bishop JA, Beswick S, Randerson-Moor J, Chang YM, Affleck P, Elliott F, et al. Serum 25-hydroxyvitamin D3 levels are associated with Breslow thickness at presentation and survival from melanoma. J Clin Oncol 2009;27:5439-44
-
(2009)
J Clin Oncol
, vol.27
, pp. 5439-5444
-
-
Newton-Bishop, J.A.1
Beswick, S.2
Randerson-Moor, J.3
Chang, Y.M.4
Affleck, P.5
Elliott, F.6
-
136
-
-
0036847390
-
Genetic testing for melanoma
-
Kefford R, Bishop JN, Tucker M, Bressac-de Paillerets B, Bianchi-Scarrá G, Bergman W, et al. Genetic testing for melanoma. Lancet Oncol 2002;3:653-4
-
(2002)
Lancet Oncol
, vol.3
, pp. 653-654
-
-
Kefford, R.1
Bishop, J.N.2
Tucker, M.3
Bressac-De Paillerets, B.4
Bianchi-Scarrá, G.5
Bergman, W.6
-
137
-
-
0032887878
-
Counseling and DNA testing for individuals perceived to be genetically predisposed to melanoma: A consensus statement of the Melanoma Genetics Consortium
-
Kefford RF, Newton Bishop JA, Bergman W, Tucker MA. Counseling and DNA testing for individuals perceived to be genetically predisposed to melanoma: A consensus statement of the Melanoma Genetics Consortium. J Clin Oncol 1999;17:3245-51
-
(1999)
J Clin Oncol
, vol.17
, pp. 3245-3251
-
-
Kefford, R.F.1
Newton Bishop, J.A.2
Bergman, W.3
Tucker, M.A.4
|